| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32570747-32570948 | Common:1; Rare:91 | ||||
| chr3:32685053-32685387 | Rare:103 | ||||
| chr3:33097098-33097279 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277311-33277499 | Common:1; Rare:52 | ||||
| chr3:33718061-33718339 | Rare:108 | ||||
| chr3:33798290-33798682 | Common:3; Rare:111 | ||||
| chr3:33798985-33799163 | Rare:56 | ||||
| chr3:36993067-36993589 | Common:2; Rare:183; Clinvar:35; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:36993727-36993833 | Rare:42 | ||||
| chr3:37243166-37243348 | Common:1; Rare:48 | ||||
| chr3:38024510-38024664 | Common:1; Rare:57 | ||||
| chr3:38029600-38029867 | Common:1; Rare:54 | ||||
| chr3:38164892-38165089 | Rare:51 | ||||
| chr3:39051983-39052053 | Common:1; Rare:29 | ||||
| chr3:39107555-39107716 | Common:3; Rare:50 |